Branched tail lipid compounds and compositions for intracellular delivery of therapeutic agents
The disclosure features novel lipids and compositions involving the same. Lipid nanoparticles (e.g., empty LNPs or loaded LNPs) include a novel lipid as well as additional lipids such as phospholipids, structural lipids, and PEG lipids. Lipid nanoparticles (e.g., empty LNPs or loaded LNPs) further including therapeutic and/or prophylactics such as RNA are useful in the delivery of therapeutic and/or prophylactics to mammalian cells or organs to, for example, regulate polypeptide, protein, or gene expression.
1. A compound of Formula (1-1):
or its N-oxide, or a salt or isomer thereof,
wherein R′ a is R′ branched or R′ cyclic ; wherein
R′ branched is
and R′ cyclic is:
and
R′ b is
wherein
denotes a point of attachment;
wherein R aγ and R bγ are each independently a C 2-12 alkyl or C 2-12 alkenyl;
R 2 and R 3 are each independently selected from the group consisting of C 1-14 alkyl and C 2-14 alkenyl;
R 4 is —(CH 2 ) 2 OH;
each R′ independently is a C 1-12 alkyl or C 2-12 alkenyl;
Y a is a C 3-6 carbocycle;
R*″ a is selected from the group consisting of C 1-15 alkyl and C 2-15 alkenyl; and
s is 2 or 3.
2. The compound of claim 1 , having the following structure:
wherein R aγ is a C 2-6 alkyl.
3. The compound of claim 2 , having the following structure:
4. The compound of claim 1 , having the following structure:
wherein R aγ and R bγ are each independently a C 2-6 alkyl.
5. The compound of claim 1 , wherein R aγ is a C 2-6 alkyl.
6. The compound of claim 1 , wherein R bγ is a C 2-6 alkyl.
7. The compound of claim 1 , wherein R 2 and R 3 are each C 8 alkyl.
8. The compound of claim 1 , wherein Y a is cyclohexyl or cyclopentyl.
9. The compound of claim 8 , wherein R*″ a is a C 2 -alkyl or C 3 -alkyl.
10. The compound of claim 2 , wherein R′ is a C 2-5 alkyl.
11. The compound of claim 3 , wherein R′ is a C 2-5 alkyl.
12. The compound of claim 4 , wherein each R′ is a C 2-5 alkyl.
13. The compound of claim 4 , wherein R bγ is a C4-6 alkyl.
14. A compound of Formula (2-1):
or its N-oxide, or a salt or isomer thereof,
wherein R′ a is R′ branched or R′ cyclic ; wherein
R′ branched is
and R′ cyclic is:
and
R′ b is:
wherein
denotes a point of attachment;
wherein R aγ and R bγ are each independently a C 2-12 alkyl or C 2-12 alkenyl;
R 2 and R 3 are each independently selected from the group consisting of C 1-14 alkyl and C 2-14 alkenyl;
R 4 is
wherein
denotes a point of attachment;
R10 is N(R) 2 ; each R is independently selected from the group consisting of C 1-6 alkyl, C 2-3 alkenyl, and H; and n2 is selected from the group consisting of 1, 2, 3, 4, 5, 6, 7, 8, 9, and 10;
each R′ independently is a C 1-12 alkyl or C 2-12 alkenyl;
Y a is a C 3-6 carbocycle;
R*″ a is selected from the group consisting of C 1-15 alkyl and C 2-15 alkenyl; and
s is 2 or 3.
15. A compound selected from:
16. An empty lipid nanoparticle (empty LNP) comprising a compound of claim 1 , a phospholipid, a structural lipid, and a PEG lipid.
17. The empty LNP of claim 16 , comprising about 40 mol % to about 60 mol % said compound, about 0 mol % to about 20 mol % phospholipid, about 30 mol % to about 50 mol % structural lipid, and about 0 mol % to about 5 mol % PEG lipid.
18. The empty LNP of claim 16 , wherein the phospholipid is selected from the group consisting of:
1,2-dilinoleoyl-sn-glycero-3-phosphocholine (DLPC), 1,2-dimyristoyl-sn-glycero-phosphocholine (DMPC), 1,2-dioleoyl-sn-glycero-3-phosphocholine (DOPC), 1,2-dipalmitoyl-sn-glycero-3-phosphocholine (DPPC), 1,2-distearoyl-sn-glycero-3-phosphocholine (DSPC), 1,2-diundecanoyl-sn-glycero-phosphocholine (DUPC), 1-palmitoyl-2-oleoyl-sn-glycero-3-phosphocholine (POPC), 1,2-di-O-octadecenyl-sn-glycero-3-phosphocholine (18:0 Diether PC), 1-oleoyl-2-cholesterylhemisuccinoyl-sn-glycero-3-phosphocholine (OChemsPC), 1-hexadecyl-sn-glycero-3-phosphocholine (C16 Ly so PC), 1,2-dilinolenoyl-sn-glycero-3-phosphocholine, 1,2-diarachidonoyl-sn-glycero-3-phosphocholine, 1,2-didocosahexaenoyl-sn-glycero-3-phosphocholine, 1,2-dioleoyl-sn-glycero-3-phosphoethanolamine (DOPE), 1,2-diphytanoyl-sn-glycero-3-phosphoethanolamine (ME 16.0 PE), 1,2-distearoyl-sn-glycero-3-phosphoethanolamine, 1,2-dilinoleoyl-sn-glycero-3-phosphoethanolamine, 1,2-dilinolenoyl-sn-glycero-3-phosphoethanolamine, 1,2-diarachidonoyl-sn-glycero-3-phosphoethanolamine, 1,2-didocosahexaenoyl-sn-glycero-3-phosphoethanolamine, 1,2-dioleoyl-sn-glycero-3-phospho-rac-(1-glycerol) sodium salt (DOPG), sphingomyelin, and mixtures thereof.
19. The empty LNP of claim 16 , wherein the structural lipid is selected from the group consisting of cholesterol, fecosterol, sitosterol, ergosterol, campesterol, stigmasterol, brassicasterol, and mixtures thereof.
20. The empty LNP of claim 16 , wherein the PEG lipid is selected from the group consisting of a PEG-modified phosphatidylethanolamine, a PEG-modified phosphatidic acid, a PEG-modified ceramide, a PEG-modified dialkylamine, a PEG-modified diacylglycerol, a PEG-modified dialkylglycerol, and mixtures thereof.
21. The empty LNP of claim 16 , wherein the PEG lipid is selected from PEG 2k -DMG and PEG-1:
and mixtures thereof.
22. A loaded lipid nanoparticle (loaded LNP), which comprises the empty LNP of claim 16 and one or more therapeutic and/or prophylactic agents.
23. The loaded LNP of claim 22 , wherein the one or more therapeutic and/or prophylactic agents is a nucleic acid.
24. The loaded LNP of claim 23 , wherein the nucleic acid is an RNA, and wherein the RNA is selected from the group consisting of a short interfering RNA (siRNA), an asymmetrical interfering RNA (aiRNA), a RNA interference (RNAi) molecule, a microRNA (miRNA), an antagomir, an antisense RNA, a ribozyme, a Dicer-substrate RNA (dsRNA), a small hairpin RNA (shRNA), a messenger RNA (mRNA), and mixtures thereof.
25. The loaded LNP of claim 24 , wherein the RNA is an mRNA.
26. A pharmaceutical composition comprising the loaded LNP of claim 22 and a pharmaceutically acceptable carrier.
27. A method of delivering a therapeutic and/or prophylactic agent to a cell within a subject, the method comprising administering to the subject the loaded LNP of claim 22 .
28. A method of specifically delivering a therapeutic and/or prophylactic agent to an organ of a subject, the method comprising administering to the subject the loaded LNP of claim 22 .
29. A method of producing a polypeptide of interest in a cell within a subject, the method comprising administering to the subject the loaded LNP of claim 25 .
30. A method of treating a disease or disorder in a subject in need thereof, the method comprising administering to the subject a therapeutically effective amount of the loaded LNP of claim 22 .